Understanding Your Laboratory Test and Results
A blood test that measures the level of 17-hydroxyprogesterone, a hormone used to screen for congenital adrenal hyperplasia (CAH) in newborns.
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Key facts at a glance
- LOINC
- 110877-8
- Short code
- 17-OHP-DBS
- Synonyms
- 17OHP Msmt DBS
- Category
- chemistry
- Sample
- serum
- Container
- Dried Blood Spot (DBS) card or serum separator tube (SST) for venous sample
- Units
- N/A
- Ref low
- 0.6
- Ref high
- 4.3
- Critical range
- — – 50 N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 0–120 years
- Method
- Immunoassay (Chemiluminescence or ELISA) or Liquid Chromatography-Tandem Mass Spectrometry (LC-MS/MS)
- CPT
- 83498
- SNOMED
- 313295004
- Specimen volume
- DBS: One complete spot (approximately 50-100 μL blood); Serum: 1-2 mL
- Stability
- DBS: Room temperature up to 7 days, refrigerated 2-8°C up to 14 days, frozen -20°C for longer storage. Serum: Refrigerated 2-8°C up to 7 days, frozen -20°C up to 30 days.
- Hemolysis max
- 50
- Lipemia max
- 100
- Icterus max
- 20
- TAT
- 24–72 hours
- Order
- routine
What is this test? This laboratory test examines a patient sample to look for specific substances, cells, or other markers that may provide information about your health.
The 17-Hydroxyprogesterone (17-OHP) test measures the amount of a hormone called 17-hydroxyprogesterone in the blood. This hormone is produced by the adrenal glands, which are small glands located on top of each kidney. The test is primarily used as part of newborn screening programs to check for a genetic condition called congenital adrenal hyperplasia (CAH).
Why is this test performed? Your clinician may order it to help evaluate symptoms, screen for a condition, monitor treatment, or check how your body is functioning over time.
This test is mainly performed on newborns as part of routine newborn screening. The goal is to detect CAH early, before symptoms develop. Congenital adrenal hyperplasia is a group of genetic disorders that affect the adrenal glands' ability to produce cortisol and sometimes aldosterone. When detected early, CAH can be managed effectively with medication, preventing serious complications such as salt-wasting crises, abnormal puberty, and growth problems.
How is the sample collected? Depending on the test, a trained healthcare professional may collect blood, urine, saliva, a swab, or another specimen using standard procedures designed to protect your comfort and safety.
For newborns, a small blood sample is typically collected by pricking the baby's heel. This is often done as part of the routine newborn screening panel, usually within 24-72 hours after birth. The blood is placed on a special filter paper and sent to a laboratory for testing. In some cases, the test may also be performed on a blood sample drawn from a vein in older children or adults who are being evaluated for CAH or related conditions.
What do the results mean? Results are interpreted using the laboratory’s reference range, your medical history, symptoms, and other findings, so an abnormal value does not always mean that you have a disease.
Normal 17-OHP levels vary by age and can differ between laboratories. Higher than normal levels may indicate congenital adrenal hyperplasia. However, a single elevated result does not confirm the diagnosis. Follow-up testing, including repeat 17-OHP measurement and possibly genetic testing, is usually needed to confirm the diagnosis. Some newborns may have temporarily elevated 17-OHP due to stress or prematurity, so clinical correlation is important.
Reference range
Reference ranges vary by age and clinical context. For newborns (3-5 days): typically <30 nmol/L; For infants and children: <3 nmol/L; Adults: 0.6-4.3 nmol/L. Consult laboratory-specific reference ranges.N/A
No special preparation required. For newborns, sample is typically collected via heel stick as part of routine newborn screening. Inform clinician of any current medications.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
The 17-OHP test is primarily used for newborn screening of classic congenital adrenal hyperplasia. Classic CAH is the most severe form and requires early treatment to prevent life-threatening salt-wasting crises in newborns. The test is also used to monitor treatment effectiveness in patients already diagnosed with CAH, helping healthcare providers adjust medication dosages. Additionally, the test may be used in older children and adults presenting with symptoms of CAH, such as early puberty, irregular periods, or excess hair growth in females.
Non-classic CAH, a milder form of the condition, may not be detected by newborn screening and might only be identified later in childhood or adulthood when symptoms appear. In these cases, the 17-OHP test may be used as a diagnostic tool along with other hormone tests to confirm the diagnosis.
Frequently asked questions
Is the 17-OHP test painful for my baby?
What happens if my baby's 17-OHP level is high?
Can CAH be treated?
Is CAH inherited?
Are there any risks associated with this test?
Sources
- 1
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- 3
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This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 10, 2026. · Read our editorial policy